ClinVar Miner

List of variants in gene ADAMTS2 reported as benign by GeneDx

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Gene type:
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Total variants: 51
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HGVS dbSNP
GRCh38/hg38 5q35.3(chr5:179342470-179506406)x3
NC_000005.10:g.179137473del
NC_000005.10:g.179345630C>G
NM_014244.5(ADAMTS2):c.1194C>T (p.Asp398=) rs2278221
NM_014244.5(ADAMTS2):c.1238+18G>A rs2278222
NM_014244.5(ADAMTS2):c.1281C>T (p.Asp427=) rs34424371
NM_014244.5(ADAMTS2):c.1383-22C>T
NM_014244.5(ADAMTS2):c.139+276A>G
NM_014244.5(ADAMTS2):c.1516-138A>G
NM_014244.5(ADAMTS2):c.1630-18T>C rs2303638
NM_014244.5(ADAMTS2):c.1776-292G>A
NM_014244.5(ADAMTS2):c.1803G>A (p.Ser601=) rs76754323
NM_014244.5(ADAMTS2):c.1908C>T (p.His636=) rs1862211
NM_014244.5(ADAMTS2):c.1951+271G>A
NM_014244.5(ADAMTS2):c.1952-319A>G
NM_014244.5(ADAMTS2):c.2028C>T (p.Asp676=) rs1972715
NM_014244.5(ADAMTS2):c.2085+266T>C
NM_014244.5(ADAMTS2):c.2085+267G>A
NM_014244.5(ADAMTS2):c.2086-190C>T
NM_014244.5(ADAMTS2):c.2209+193T>C
NM_014244.5(ADAMTS2):c.2291-8A>G rs140401199
NM_014244.5(ADAMTS2):c.2480G>A (p.Arg827Gln) rs35445112
NM_014244.5(ADAMTS2):c.2532C>T (p.Asp844=) rs2303644
NM_014244.5(ADAMTS2):c.2618-319T>C
NM_014244.5(ADAMTS2):c.2730A>G (p.Pro910=) rs6869261
NM_014244.5(ADAMTS2):c.2750+284C>T
NM_014244.5(ADAMTS2):c.2958+87G>A
NM_014244.5(ADAMTS2):c.2959-16G>A rs6863024
NM_014244.5(ADAMTS2):c.2959-17C>T rs2303641
NM_014244.5(ADAMTS2):c.2959-194T>G
NM_014244.5(ADAMTS2):c.3088+319_3088+320insGCCTGTGTGAGTGGGGGGT
NM_014244.5(ADAMTS2):c.3178+203_3178+213del
NM_014244.5(ADAMTS2):c.321T>C (p.Ser107=) rs2271212
NM_014244.5(ADAMTS2):c.3480C>A (p.Ala1160=) rs34437036
NM_014244.5(ADAMTS2):c.3529C>T (p.Pro1177Ser) rs1054480
NM_014244.5(ADAMTS2):c.47_49TGC[7] (p.Leu23del) rs568040559
NM_014244.5(ADAMTS2):c.47_49TGC[9] (p.Leu23dup) rs568040559
NM_014244.5(ADAMTS2):c.534+283G>T
NM_014244.5(ADAMTS2):c.534+50T>C
NM_014244.5(ADAMTS2):c.534+9G>C rs2271213
NM_014244.5(ADAMTS2):c.689-262T>A
NM_014244.5(ADAMTS2):c.689-289G>A
NM_014244.5(ADAMTS2):c.701A>G (p.Asp234Gly) rs59567206
NM_014244.5(ADAMTS2):c.722G>A (p.Arg241His) rs11750821
NM_014244.5(ADAMTS2):c.733G>A (p.Val245Ile) rs398829
NM_014244.5(ADAMTS2):c.786G>A (p.Ala262=) rs423552
NM_014244.5(ADAMTS2):c.858C>T (p.His286=) rs66565583
NM_014244.5(ADAMTS2):c.891+33C>G
NM_014244.5(ADAMTS2):c.892-185G>A
NM_014244.5(ADAMTS2):c.936C>T (p.Asn312=) rs35462609
NM_014244.5(ADAMTS2):c.976-161G>T

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